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nsv5549762

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:27

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 119 SVs from 24 studies. See in: genome view    
Submitted genomic70,159,242-70,159,268Question Mark
Overlapping variant regions from other studies: 119 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):71,071,477-71,071,503Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5549762Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr870,159,24270,159,268
nsv5549762RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr871,071,47771,071,503

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17735820insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17735820Submitted genomicNC_000008.11:g.701
59242_70159268ins7
8
GRCh38 (hg38)NC_000008.11Chr870,159,24270,159,268
nssv17735820RemappedPerfectNC_000008.10:g.710
71477_71071503ins7
8
GRCh37.p13First PassNC_000008.10Chr871,071,47771,071,503

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv177358200.002146390
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